No association between dysplasminogenemia with p.Ala620Thr mutation and atypical hemolytic uremic syndrome.

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Bibliographic Details
Title: No association between dysplasminogenemia with p.Ala620Thr mutation and atypical hemolytic uremic syndrome.
Authors: Miyata T; Department of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center, 5-7-1 Fujishirodai, Suita, Osaka, 565-8565, Japan. miyata@ncvc.go.jp., Uchida Y; Department of Molecular Pathogenesis, National Cerebral and Cardiovascular Center, Suita, Japan., Yoshida Y; Division of Nephrology and Endocrinology, University of Tokyo School of Medicine, Tokyo, Japan., Kato H; Division of Nephrology and Endocrinology, University of Tokyo School of Medicine, Tokyo, Japan., Matsumoto M; Department of Blood Transfusion Medicine, Nara Medical University, Kashihara, Japan., Kokame K; Department of Molecular Pathogenesis, National Cerebral and Cardiovascular Center, Suita, Japan., Fujimura Y; Japanese Red Cross Kinki Blood Center, Ibaraki, Japan., Nangaku M; Division of Nephrology and Endocrinology, University of Tokyo School of Medicine, Tokyo, Japan.
Source: International journal of hematology [Int J Hematol] 2016 Aug; Vol. 104 (2), pp. 223-7. Date of Electronic Publication: 2016 May 18.
Publication Type: Journal Article
Journal Info: Publisher: Springer Japan Country of Publication: Japan NLM ID: 9111627 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1865-3774 (Electronic) Linking ISSN: 09255710 NLM ISO Abbreviation: Int J Hematol Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1865-3774
DOI:10.1007/s12185-016-2021-3